lecture 4 Flashcards

1
Q

observational studies

A

observe the outcomes without intervening to affect them

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2
Q

experimental studies

A

researcher manipulates the exposure (usually drug or tx) to compare to standard of care

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3
Q

types of observational studies

A

cohort
case control
cross sectional

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4
Q

cohort studies

A

subjects are selected based on exposure status

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5
Q

prospective cohort study

A

compares disease prevalence in the exposed and unexposed

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6
Q

retrospective cohort study

A

begin with exposure of interest and probe back for exposure info

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7
Q

advantages of cohort studes

A

maintain temporary sequence

GOOD FOR RARE EXPOSURES, RAPIDLY FATAL DZ

can study multiple dz/outcomes from given exposure

can calculate incidence in exposed vs unexposed

minimizes error (prospective)

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8
Q

which type of study is good for rare EXPOSURES, fatal diseases

A

cohort

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9
Q

which type of study can calculate incidence among exposed and unexposed

A

cohort

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10
Q

disadvantages of cohort studies

A

expensive

inefficient for rare disease

long follow up

secular trends may influence behavior/characterstics over time

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11
Q

are cohort studies good for rare diseases

A

NO, good for rare EXPOSURES

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12
Q

how are subjects selected for case-control studies

A

disease status

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13
Q

how should cases/controls differ

A

ONLY IN PAST EXPOSURE

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14
Q

can temporality be assessed in case-control studies

A

no

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15
Q

can case-control demonstrate risk indicators or risk factors

A

indicators only (no temporal relationship)

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16
Q

cases and controls must

A

have had an EQUAL CHANCE OF BEING EXPOSED

17
Q

which type of study is good for rare diseases

A

case-control

18
Q

advantage of case-control

A

efficient for rare diseases

good time/money

diseases with long latency period

evaluate multiple exposures

19
Q

can a case control study directly compute incidence of disease in exposed and non-exposed persons

A

NO

20
Q

disadvantages of case-control

A

temporal relationship cannot be establishsed

prone to errors in selecting of cases/controls

not optimal for rare exposures

21
Q

cross sectional studies

A

selection of subjects based on neither exposure or dz status

22
Q

do cross sectional studies need explained etiologic objectives

A

no

23
Q

advantages of cross sectional

A

sampling and analytic methods provide for statistically valid inference to populations

exposure and dz are assessed at individual level

24
Q

disadvantage of cross sectional

A

temporality cannot be assessed

25
Q

what is the primary purpose of randomization in RCT

A

minimizing of confounding

26
Q

single blinded

A

participant does not know but investigators do know tx assignment

27
Q

what is information bias

A

drawing different conclusions depending on their knowledge of which study arm particular participant is in

28
Q

what is selection bias

A

study recruiters can be eager to recruit “sick persons” into experimental arm

29
Q

meta analysis

A

combined analysis of data from different studies following strict guidelines